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nsv5487693

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,236

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 198 SVs from 62 studies. See in: genome view    
Submitted genomic93,911,048-93,915,283Question Mark
Overlapping variant regions from other studies: 198 SVs from 62 studies. See in: genome view    
Remapped(Score: Perfect):93,540,360-93,544,595Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5487693Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr793,911,04893,915,283
nsv5487693RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr793,540,36093,544,595

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17000383deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17000383Submitted genomicNC_000007.14:g.939
11048_93915283del
GRCh38 (hg38)NC_000007.14Chr793,911,04893,915,283
nssv17000383RemappedPerfectNC_000007.13:g.935
40360_93544595del
GRCh37.p13First PassNC_000007.13Chr793,540,36093,544,595

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17000383<0.00126402
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